EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS120-02366 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr16:22201180-22203530 
Target genes
Number: 7             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs145049847chr1622202002hg19
TF binding sites/motifs
Number: 22             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr16:22202295-22202306CCTTCCCGCCC-6.62
EWSR1-FLI1MA0149.1chr16:22201270-22201288GTAAGGAAGAAAGGAAGA+6.81
KLF13MA0657.1chr16:22201894-22201912TGGCCACGCCCCTATCTA+6.26
KLF14MA0740.1chr16:22202286-22202300AGCCACGCCCCTTC+6.1
KLF14MA0740.1chr16:22201895-22201909GGCCACGCCCCTAT+6.29
KLF16MA0741.1chr16:22202164-22202175GCCCCGCCCCC+6.02
KLF16MA0741.1chr16:22202657-22202668GCCCCGCCCCC+6.02
KLF5MA0599.1chr16:22201948-22201958GCCCCGCCCC+6.02
KLF5MA0599.1chr16:22202164-22202174GCCCCGCCCC+6.02
KLF5MA0599.1chr16:22202657-22202667GCCCCGCCCC+6.02
Klf12MA0742.1chr16:22202071-22202086GACCACGCCCTTGAC+6.18
Klf12MA0742.1chr16:22201895-22201910GGCCACGCCCCTATC+6.39
SP1MA0079.4chr16:22202161-22202176CTAGCCCCGCCCCCG+6.13
SP1MA0079.4chr16:22201893-22201908CTGGCCACGCCCCTA+6.41
SP1MA0079.4chr16:22202654-22202669CTGGCCCCGCCCCCT+6.57
SP1MA0079.4chr16:22202284-22202299ATAGCCACGCCCCTT+6.5
SP2MA0516.2chr16:22202344-22202361CTCTGTCCCGCCCCCTG+6.05
SP2MA0516.2chr16:22202653-22202670CCTGGCCCCGCCCCCTC+6.09
SP4MA0685.1chr16:22202161-22202178CTAGCCCCGCCCCCGTT+6.66
SP4MA0685.1chr16:22202284-22202301ATAGCCACGCCCCTTCC+6.93
SP4MA0685.1chr16:22201893-22201910CTGGCCACGCCCCTATC+6.9
SP4MA0685.1chr16:22202654-22202671CTGGCCCCGCCCCCTCC+7.25
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00683chr16:22199332-22208185Adipose_Nuclei
SE_01979chr16:22200329-22204592Aorta
SE_10487chr16:22199321-22204649CD19_Primary
SE_11249chr16:22197627-22207934CD20
SE_11977chr16:22199271-22204610CD3
SE_14827chr16:22199054-22204871CD4_Memory_Primary_7pool
SE_15511chr16:22199096-22204729CD4_Memory_Primary_8pool
SE_16039chr16:22199414-22204303CD4_Naive_Primary_7pool
SE_16474chr16:22199243-22204501CD4_Naive_Primary_8pool
SE_16960chr16:22199331-22204777CD4p_CD225int_CD127p_Tmem
SE_17421chr16:22197856-22207948CD4p_CD25-_CD45RAp_Naive
SE_17990chr16:22197681-22205577CD4p_CD25-_CD45ROp_Memory
SE_20295chr16:22199376-22204902CD56
SE_21095chr16:22199644-22204726CD8_Memory_7pool
SE_21701chr16:22199330-22204547CD8_Naive_7pool
SE_22039chr16:22199259-22204858CD8_Naive_8pool
SE_22558chr16:22198010-22204854CD8_primiary
SE_27459chr16:22199727-22204779Esophagus
SE_29992chr16:22199834-22204871Fetal_Muscle
SE_42904chr16:22199330-22204886Lung
SE_48301chr16:22199834-22204912Psoas_Muscle
SE_49024chr16:22199991-22204825Right_Atrium
SE_51662chr16:22199489-22204834Skeletal_Muscle
SE_54110chr16:22199445-22204828Spleen
SE_61402chr16:22199511-22230924HBL1
SE_63046chr16:22199134-22211533Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr162220259622202946
Number: 1             
IDChromosomeStartEnd
GH16I022187chr162219893022205452
Enhancer Sequence
TCTTAGGGAC CAAGGAGTTA AATAGGGTGC GAATTCAGCG GGGCTGGAGG GGGCGACGCA 60
AAGGCGGCAC CCTCCAATAA AAATGAACAT GTAAGGAAGA AAGGAAGACC TCTCTAATGA 120
GGGCATCGCA GGAGCAAGAC GCTGCACTCG GGTCCTTTTA AATCACTATG TAATGGAGGG 180
GAAATCCCTG CCCTCTCTTT TCCCTTTCCG TAAACAACGA AGTAGAGGAT GTCCTCCTCC 240
CACGAGGCCC GCCCTCGGAT GCCCCGCCTG TCCCCGCAGG TGCGCAGCGT GGCCGTGACG 300
CACACCTTCC AGATAGCCAA GGCCCGCGCC CAGCTCGGCT ACGCGCCGGA TAAGTTTAGG 360
TTCGCCGACG CCGTGGAGCT ATACGTGCAG TCCACGACCC GGCGGCCCCG CGGCTCCACG 420
GCGCGGACCC TCCTGCGCCT GCTGCTCAGG CTGCTGCTGT TCCTCGGCTT GCTCGCCCTG 480
GCCCTGCACT TCCTAGGCCT GCAGCCTCTG CACGCCGCCG TGGAGCGCCT GTGACCGTCC 540
GCCGTCCGCC GCCCGCTAGG GTCGGCCCCG CTGCACCCTC GCCCACGCCC GGCTCCCTGG 600
GCTTGTACCA GCCCCTGCCC CGCCTTCTGG GTTTGAGCGC GCCTCCGCTC CGCCCCTTGA 660
ATCCTGGTCA CGCCCCCGAG CCGCTCTCCA GACCTAGCCC GGACCGCCGA CTTCTGGCCA 720
CGCCCCTATC TACTCCCAGA CCTTGCCTTG CGCCCTTCCT GTGTTTTGGC CCCGCCCCTG 780
TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC TCCGCCCCCT GAATCCTGGC 840
CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT TTCCATGTTT TGACCACGCC 900
CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC TCACTGATTT CCTGGCCTAG 960
CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT ATAACCCCGC CCCTGCTTCA 1020
CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG CCTAGTCCTG AGCCGCTCTC 1080
CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC CCGCCCTTCC ATGTTTGGGC 1140
ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT GAATCTTTCC TACGTCCATG 1200
ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC CTCCGGCCTG TCCGGTTTCT 1260
GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC CTTCTCCTAG TCCCTGCCCA 1320
GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG CCCCCTTTCT GGTCCTCCCC 1380
GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT GTCCTTGCTC CTGCCTCTGG 1440
ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC CCGCCCCCTC CCTCTCTGGC 1500
TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC CGGAACCAGG CTGCCGCGTC 1560
GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT TTGCGCCGTC GGCTGCTGCT 1620
CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG TTCTGGGCTT CTCATTCACA 1680
CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG AGACTCAAGC TTCTGCCGAG 1740
CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG CATAGTAAGC ACAGGTTTTA 1800
GTACCAGAAA GAGCATGAAA AATTTAAAAA AAAAAACTCT TAAAATAATT GGATGTCTCG 1860
ATGAAGTACC AATAAAGCTA TAATGGGAAA AATAGAGTTT AGTTGGTTAT ATTTTATGAT 1920
TTAGTACTGT TTCTATTTAT TAATTAGAGG TAGTGGTAAT CACCATAATC TTTAAAGTTT 1980
AAGGTCACGA AACTTCTTTA TCTAGCCCTG CTCTCCACAG AAACTTCGCC TCCTATCATC 2040
TTGGTATCAG TTATCAGTTG TAAGTACCAA GACATCAGTG TGTAAATACA ACCATGTATA 2100
GATCATAATA TGCACACGTG GGACTGGCAG AGAAGAAAAG CACCACAAGC CTGAGGTGGA 2160
TGGGATCGAA AGGGCTCATC AGAACCAACA TGGCCACCGC AGTGTGTGTC CCACTCTGCT 2220
GAACAAGGTG AGCAGTTTGG GAAGGAGCTA AAAAAAAATG TATGCTCCTC TCTGCTAGGC 2280
TGAATTTTAT GTGTGTATAT AATTTTTGAA AGAATAATAA TCCTATGTCT GTTTAATGCT 2340
TGACAGTGTA 2350